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Man Li
@amai911122
Clinical Research Associate GCP Clinical Trial Documentation Specialist
China
English, Chinese
About me
I am a Clinical Research Associate (CRA) with 5 years of experience across global pharmaceutical and CRO studies - oncology, diabetes, dermatology, ophthalmology and more. I help international clients prepare accurate, compliance-ready clinical and pharmaceutical documents.
Services: clinical trial SOPs (GCP/GDP), GMP docs (BMR/BPR, validation protocols), study documents (IB, ICF, CSR summaries), medical content writing. Bachelor's in Pharmaceutical Engineering, Shenyang Pharmaceutical University.
I respond fast and treat every document as if it were going to a regulatory authority.
Skills
Man Li
Offline •
Average response time: 1 hour
See my services
Technical Writing
I will write gcp clinical trial protocols, sops, icfs, and csrs
Research & Summaries
I will write clinical research manuscripts, systematic reviews, and congress abstracts
